|
771
|
|
|
Pleckstrin homology and RhoGEF domain containing G5 |
ARHGEF45, CMTRIC, DSMA4, GEF720, HMNR4, Syx, Tech |
Atrophy, Charcot-marie-tooth disease, Color vision deficiency, Dejerine-sottas disease, Distal spinal muscular atrophy, Motor neuron disease, Hypertrophic neuropathy, Amyotrophic lateral sclerosis, Multiple sclerosis, Neuromuscular diseases, Neuronopathy, distal hereditary motor, Peripheral neuropathy, Peroneal muscle atrophy, Polycystic ovary syndrome, Roussy-levy syndrome, Hereditary spastic paraplegia, Spinal muscular atrophyView all (2 more) |
|
772
|
|
|
Parathyroid hormone 1 receptor |
EKNS, PFE, PTHR, PTHR1 |
Brachydactyly, Hepatocellular carcinoma, Chondrodysplasia, Congenital cartilage disorder, Connective tissue disease, Desbuquois syndrome, Gout, Hyperparathyroidism, Lung disease, Metaphyseal chondrodysplasia, Osteochondrodysplasias, Pseudohypoparathyroidism, Rickets, Diabetes mellitus, type 2 |
|
773
|
|
|
Parathyroid hormone 2 receptor |
PTHR2 |
|
|
774
|
|
|
Protein tyrosine kinase 2 |
FADK, FADK 1, FAK, FAK1, FRNK, PPP1R71, p125FAK, pp125FAK |
Rheumatoid arthritis, Eczema, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Autism, Byzanthine arch palate, Hepatocellular carcinoma, Squamous cell carcinoma, Cardioembolic stroke, Malocclusion, Color vision deficiency, Glioblastoma, Hearing loss, Hypertension, Intestinal infectious disease, Mouth neoplasm, Willis-ekbom disease, Substance abuseView all (4 more) |
|
775
|
|
|
Proline rich 12 |
KIAA1205, NOC |
Autism, Hodgkin lymphoma, Intellectual developmental disorder, Myositis, Neurodevelopmental disorders, Neuroocular syndrome, Rheumatoid arthritis, Skin cancer, Skin neoplasm, Systemic lupus erythematosus, Systemic sclerosis |
|
776
|
|
|
Pleckstrin homology and RhoGEF domain containing G1 |
ARHGEF41 |
Alzheimer disease, Cardiovascular disease, Coronary artery disease, Hypertension, Major depressive disorder, Myocardial infarction, Obesity, Panic disorder, Periventricular leukomalacia, Diabetes mellitus, type 2, Uterine polyp |
|
777
|
|
|
Protocadherin 19 |
DEE9, EFMR, EIEE9 |
Autism, Developmental and epileptic encephalopathy, Dravet syndrome, Epilepsy, Female restricted epilepsy with intellectual disability, Rolandic epilepsy, Seizure, Global developmental delay, Intellectual developmental disorder, Seizures, Strabismus, X-linked complex neurodevelopmental disorder, X-linked intellectual disability |
|
778
|
|
|
Protein tyrosine kinase 7 (inactive) |
CCK-4, CCK4 |
|
|
779
|
|
|
Prothymosin alpha |
TMSA |
|
|
780
|
|
|
Protocadherin 10 |
OL-PCDH, PCDH19 |
|
